From Surf Wiki (app.surf) — the open knowledge base
4-Bromoaniline
4-Bromoaniline is a compound where an aniline molecule is substituted with a bromine atom on the para position. Commercially available, this compound may be used as a building block, e.g. in the preparation of monobrominated biphenyl via the Gomberg–Bachmann reaction.
Preparation
4-Bromoaniline can be made by reacting acetyl chloride-protected aniline with bromine.
Reactions
One laboratory route to 1-bromo-4-iodobenzene involves the Sandmeyer reaction. 4-Bromoaniline is treated with concentrated sulfuric acid and sodium nitrite, then potassium iodide.
References
References
- [http://www.chemblink.com/products/106-40-1.htm 4-Bromoaniline], Chemblink.com
- [[Moses Gomberg. (1941). "p-Bromobiphenyl".
- (15 January 2009). "Synthesis, Optical, and Electronic Properties of Soluble Poly-p-phenylene Oligomers as Models for Molecular Wires". [[Journal of the American Chemical Society]].
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about 4-Bromoaniline — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report